K223078Substantially Equivalent
Atellica® CH Diazo Direct Bilirubin (D_DBil)
Siemens Healthcare Diagnostics Inc., Newark DE / Traditional, Substantially Equivalent
K223078 is the FDA 510(k) clearance record for Atellica® CH Diazo Direct Bilirubin (D_DBil), a class II device, cleared for Siemens Healthcare Diagnostics, Inc. on under FDA product code CIG (Diazo Colorimetry, Bilirubin). FDA records list 1,204 510(k) clearances for Siemens Healthcare Diagnostics, Inc., from to . As of , FDA records show no recalls naming K223078.
Clearance record
- Decision date
- Received
- (255 days to decision)
- Product code
- CIG Diazo Colorimetry, Bilirubin
- Regulation
- 21 CFR 862.1110
- Device class
- Class II
- Review panel
- Clinical Chemistry
- Applicant
- Siemens Healthcare Diagnostics, Inc. 500 Gbc Dr.,, Newark DE
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code CIG
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 1 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
